Bismuth Coordinates with Iodine Atoms to Form Chemical Bonds for Existing Stabilization in Boron Glass.

Stabilizing radioactive iodine in boron glass for disposal was the ultimate goal of this study. In this study, bismuth was used near a monument. Thermogravimetric analysis showed that bismuth could remarkably stabilize iodine atoms in boron glass (only 3.74% of the mass was lost at 850 °C). Scanning electron microscopy-energy dispersive spectrometry images showed that most of the AgI was uniformly immobilized in the glass network. X-ray photoelectron spectrometry and NMR results confirmed the change in the coordination number of boron in the samples. The density functional theory calculation helped to understand the reason for the stable presence of iodine in boron glass. Iodine atoms were difficult to bond directly with boron atoms but tended to bond with bismuth atoms. From the spatial distribution of the structural molecular orbitals, it was observed that the bismuth atom releases electrons when stimulated, and the iodine atom needs to gain an electron to reach stability. At a low treatment temperature of 550 °C, the maximum density of the immobilized sample containing bismuth is 2.42 g·cm-3, and its iodine leaching rate at day 7 can be as low as 3.77 × 10-6 g·m-2·d-1. This study provides a way to improve the properties of boron glass microscopically in the future.

Correction: Plasma-induced grafting of polyacrylamide on graphene oxide nanosheets for simultaneous removal of radionuclides.

Correction for 'Plasma-induced grafting of polyacrylamide on graphene oxide nanosheets for simultaneous removal of radionuclides' by Wencheng Song et al., Phys. Chem. Chem. Phys., 2015, 17, 398-406.

New Insight into GO, Cadmium(II), Phosphate Interaction and Its Role in GO Colloidal Behavior.

This study establishes the relationship between the graphene oxide (GO) colloidal behavior and the co-adsorption of Cd(II) and phosphate (P(V)) on GO. Results reveal that the interactions among GO, Cd(II), and P(V) exhibit a significant dependence on solution chemistry and addition sequences and that these interactions subsequently affect the GO colloidal behavior. The GO aggregation is pH-dependent at pH < 4.0 and depends apparently on the binding ability of Cd(II) to GO at pH > 4.0. When the components were added simultaneously, the presence of P(V) enhances the GO binding capacity toward Cd(II), confirmed by theoretical calculation, resulting in the greater destabilizing influence of Cd(II) + P(V) on GO than Cd(II) at pH 3.0-9.5, while the formation of Cd3(PO4)2 precipitate leads to a lower destabilizing influence of Cd(II) + P(V) on GO than Cd(II) at pH > 9.5. Both pH and addition sequence affect the destabilizing ability of Cd(II) + P(V). These new insights are expected to provide valuable information not only for the application of GO as a potential adsorbent in multicomponent systems for heavy metal ion and oxyanion co-removal but also for the fate and risk assessment of GO after serving as heavy metal ion and oxyanion carrier.

Plasma-induced grafting of polyacrylamide on graphene oxide nanosheets for simultaneous removal of radionuclides.

Polyacrylamide (PAM) grafted graphene oxide (denoted as PAM/GO) was synthesized by the plasma-induced polymerization technique and applied as an adsorbent for the simultaneous removal of radionuclides from radioactive wastewater. The interactions of PAM/GO with the radionuclides U(vi), Eu(III) and Co(II) were studied, along with their sorption kinetics. The results indicated that radionuclide sorption on PAM/GO was affected by the solution pH and ionic strength. The maximum sorption capacities of U(VI), Eu(III) and Co(II) on PAM/GO (0.698, 1.245 and 1.621 mmol g(-1), respectively) at pH = 5.0 ± 0.1 and T = 295 K were much higher than those of radionuclides on GO and other adsorbents. The thermodynamic data (ΔH(0), ΔS(0) and ΔG(0)) calculated from the temperature-dependent sorption isotherms suggested that the sorption of radionuclides on PAM/GO was a spontaneous and endothermic process. These results indicate that PAM/GO is a promising material for the control of radionuclide pollution.

Design of Chitosan-Grafted Carbon Nanotubes: Evaluation of How the -OH Functional Group Affects Cs+ Adsorption.

In order to explore the effect of -OH functional groups in Cs+ adsorption, we herein used the low temperature plasma-induced grafting method to graft chitosan onto carbon nanotubes (denoted as CTS-g-CNTs), as raw-CNTs have few functional groups and chitosan has a large number of -OH functional groups. The synthesized CTS-g-CNT composites were characterized using different techniques. The effect of -OH functional groups in the Cs+ adsorption process was evaluated by comparison of the adsorption properties of raw-CNTs with and without grafting chitosan. The variation of environmental conditions such as pH and contact time was investigated. A comparison of contaminated seawater and simulated groundwater was also evaluated. The results indicated that: (1) the adsorption of Cs+ ions was strongly dependent on pH and the competitive cations; (2) for CNT-based material, the -OH functional groups have a positive effect on Cs+ removal; (3) simulated contaminated groundwater can be used to model contaminated seawater to evaluate the adsorption property of CNTs-based material. These results showed direct observational evidence on the effect of -OH functional groups for Cs+ adsorption. Our findings are important in providing future directions to design and to choose effective material to remedy the removal of radioactive cesium from contaminated groundwater and seawater, crucial for public health and the human social environment.

Effect of silicate on the formation and stability of Ni-Al LDH at the γ-Al2O3 surface.

The formation of mixed metal precipitates has been identified as a significant mechanism for the immobilization and elimination of heavy metal ions. Silicate is present in natural systems ubiquitously, which may interfere with metal uptake on the mineral surface and thereby influences the solubility of the precipitate. Herein, kinetic sorption and dissolution experiments combined with extended X-ray absorption fine structure spectroscopy (EXAFS) were performed to elucidate the effect of silicate on the formation of Ni precipitates at the γ-Al2O3 surfaces. The uptake of Ni on γ-Al2O3 decreased with increasing amounts of silicate coated onto the γ-Al2O3 surface. Results of EXAFS analyses suggested the formation of Ni-Al layered double hydroxide (LDH) phases. The surface coating of silicate on γ-Al2O3 reduced Al release and finally resulted in a high Ni:Al ratio due to a lower extent of Al substitution into the precipitates. The presence of silicate prevented the growth of the precipitates and led to the formation of less stable Ni-Al LDH. The influence of silicate on the precipitate formation provided the evidence for the growth relationship between the precipitate and mineral substrate in the real environment. Increased rates of proton-promoted dissolution of Ni surface precipitates were mainly attributed to higher Ni:Al ratios in Ni-Al LDH precipitates formed in the presence of silicate.

Impact of Al2O3 on the aggregation and deposition of graphene oxide.

To assess the environmental behavior and impact of graphene oxide (GO) on living organisms more accurately, the aggregation of GO and its deposition on Al2O3 particles were systematically investigated using batch experiments across a wide range of solution chemistries. The results indicated that the aggregation of GO and its deposition on Al2O3 depended on the solution pH and the types and concentrations of electrolytes. MgCl2 and CaCl2 destabilized GO because of their effective charge screening and neutralization, and the presence of NaH2PO4 and poly(acrylic acid) (PAA) improved the stability of GO with the increase in pH values as a result of electrostatic interactions and steric repulsion. Specifically, the dissolution of Al2O3 contributed to GO aggregation at relatively low pH or high pH values. Results from this study provide critical information for predicting the fate of GO in aquatic-terrestrial transition zones, where aluminum (hydro)oxides are present.

Elimination of uranium pollution from coastal nuclear power plant by marine microorganisms: Capability and mechanism.

Uranium is one of the sensitive radionuclides in the wastewater of nuclear powers. Due to the fact that nuclear powers are mainly located in coastal areas, the elimination of uranium (U(VI)) pollution from coastal nuclear power is ultimately rely on marine microorganisms. The fixing of U(VI) on V. alginolyticus surface or converting it into sediments is an effective elimination strategy for U(VI) pollution. In this work, typical marine microorganism V. alginolyticus was used to evaluate the elimination of U(VI) pollution by marine microorganisms. Effects of solution conditions (such as pH, temperature, and bacterium concentrations) on the physicochemical properties and elimination capabilities of V. alginolyticus were studied in detail. FT-IR, XPS and XRD results reveal that COOH, NH2, OH and PO4 on V. alginolyticus were main functional groups for U(VI) elimination and formed (UO2)3(PO4)2·H2O. The elimination of U(VI) by V. alginolyticus includes two stages of adsorption and biomineralization. The theoretical maximum adsorption capacity (Cs,max) of V. alginolyticus for U(VI) can reach up to 133 mg/g at pH 5 and 298 K, and the process reached equilibrium in 3 h. Results show that V. alginolyticus play important role in the elimination of U(VI) pollution in seawater.

Application of Natural Antibacterial Plants in the Extraction of Uranium from Seawater.

Marine biofouling directly affects the performance and efficiency of uranium (U(VI)) extraction from seawater. Compared to traditional chemical methods, natural plant extracts are generally biodegradable and nontoxic, making them an environmentally friendly alternative to synthetic chemicals in solving the marine biofouling problem. The effectiveness of natural antibacterial plants (i.e., pine needle, peppermint, Acorus gramineus Soland, Cacumen platycladi, and wormwood) in solving the marine biofouling problem was evaluated in this work. Experimental results showed that natural antibacterial plants could kill Vibrio alginolyticus in solution and effectively solve the marine biofouling problem of U(VI) extraction. To improve the adsorption capacity of natural plants for U(VI) in seawater, poly(vinylphosphonic acid) (PVPA) was modified on natural antibacterial plant surfaces by irradiation grafting technology. PVPA and natural antibacterial plants work as active sites and base materials for the U(VI) extraction material, respectively. The recovery performance of PVPA/pine needle for U(VI) was preliminarily studied. Results show that the adsorption of U(VI) on PVPA/pine needle follows pseudo-second-order and Langmuir models, and the maximum adsorption capacity is 111 mg/g at 298 K and pH 8.2.

Highly efficient enrichment of radionuclides on graphene oxide-supported polyaniline.

Graphene oxide-supported polyaniline (PANI@GO) composites were synthesized by chemical oxidation and were characterized by SEM, Raman and FT-IR spectroscopy, TGA, potentiometric titrations, and XPS. The characterization indicated that PANI can be grafted onto the surface of GO nanosheets successfully. The sorption of U(VI), Eu(III), Sr(II), and Cs(I) from aqueous solutions as a function of pH and initial concentration on the PANI@GO composites was investigated. The maximum sorption capacities of U(VI), Eu(III), Sr(II), and Cs(I) on the PANI@GO composites at pH 3.0 and T = 298 K calculated from the Langmuir model were 1.03, 1.65, 1.68, and 1.39 mmol·g(-1), respectively. According to the XPS analysis of the PANI@GO composites before and after Eu(III) desorption, nitrogen- and oxygen-containing functional groups on the surface of PANI@GO composites were responsible for radionuclide sorption, and that radionuclides can hardly be extracted from the nitrogen-containing functional groups. Therefore, the chemical affinity of radionuclides for nitrogen-containing functional groups is stronger than that for oxygen-containing functional groups. This paper focused on the application of PANI@GO composites as suitable materials for the preconcentration and removal of lanthanides and actinides from aqueous solutions in environmental pollution management in a wide range of acidic to alkaline conditions.

Application of poly(vinylphosphonic acid) modified poly(amidoxime) in uptake of uranium from seawater.

To enhance the anti-biofouling properties and adsorption capability of poly(amidoxime) (PAO), vinylphosphonic acid (VPA, CH2[double bond, length as m-dash]CH-PO3H2) was polymerized on poly(acrylonitrile) (PAN) surface by plasma technique, followed by amidoximation treatment to convert the cyano group (-C[triple bond, length as m-dash]N) into an amidoxime group (AO, -C(NH2)[double bond, length as m-dash]N-OH). The obtained poly(vinylphosphonic acid)/PAO (PVPA/PAO) was used as an adsorbent in the uptake of U(vi) from seawater. The effect of environmental conditions on the anti-biofouling property and adsorption capability of PVPA/PAO for U(vi) were studied. Results show that the modified PVPA enhances the anti-biofouling properties and adsorption capability of PAO for U(vi). The adsorption process is well described by the pseudo-second-order kinetic model and reached equilibrium in 24 h. Adsorption isotherms of U(vi) on PVPA/PAO can be well fitted by the Langmuir model, and the maximum adsorption capability was calculated to be 145 mg g-1 at pH 8.2 and 298 K. Experimental results highlight the application of PVPA/PAO in the extraction of U(vi) from seawater.

Application of poly(amidoxime)/scrap facemasks in extraction of uranium from seawater: from dangerous waste to nuclear power.

To effectively kill microorganisms on scrap facemasks (FMs) surface and provide new material for extracting uranium (U(VI)) from seawater, scrap FMs was treated by N2 capacitance coupled (CCP) plasma and modified with polyamidoxime (PAO). The obtained PAO/FMs was well characterized and applied as an adsorbent in the extraction of U(VI) from seawater. The effects of environmental conditions on the adsorption capability of PAO/FMs for U(VI) were briefly studied. Results showed that plasma technique can synchronously kill microorganisms and induce acrylonitrile (AN) polymerization on FMs surface. The prepared PAO/FMs presented excellent adsorption capability for U(VI). The experimental results highlighted the application of plasma technique in the management of scrap FMs, and PAO/FMs in the extraction of U(VI) from seawater.

Retraction: A carboxymethyl cellulose modified magnetic bentonite composite for efficient enrichment of radionuclides.

[This retracts the article DOI: 10.1039/C6RA10990J.].

Mutual effects of Pb(II) and humic acid adsorption on multiwalled carbon nanotubes/polyacrylamide composites from aqueous solutions.

This paper examines the adsorption of Pb(II) and a natural organic macromolecular compound (humic acid, HA) on polyacrylamide (PAAM) -grafted multiwalled carbon nanotubes (denoted as MWCNTs/PAAM), prepared by an N(2)-plasma-induced grafting technique. The mutual effects of HA/Pb(II) on Pb(II) and HA adsorption on MWCNTs/PAAM, as well as the effects of pH, ionic strength, HA/Pb(II) concentrations, and the addition sequences of HA/Pb(II) were investigated. The results indicated that Pb(II) and HA adsorption were strongly dependent on pH and ionic strength. The presence of HA led to a strong increase in Pb(II) adsorption at low pH and a decrease at high pH, whereas the presence of Pb(II) led to an increase in HA adsorption. The adsorbed HA contributed to modification of adsorbent surface properties and partial complexation of Pb(II) with the adsorbed HA. Different effects of HA/Pb(II) concentrations and addition sequences on Pb(II) and HA adsorption were observed, indicating different adsorption mechanisms. After adsorption of HA on MWCNTs/PAAM, the adsorption capacity for Pb(II) was enhanced at pH 5.0; the adsorption capacity for HA was also enhanced after Pb(II) adsorption on MWCNTs/PAAM. These results are important for estimating and optimizing the removal of metal ions and organic substances by use of MWCNT/PAAM composites.

Transformation details of poly(acrylonitrile) to poly(amidoxime) during the amidoximation process.

During the amidoximation process, transformation details of poly(acrylonitrile) (PAN) to poly(amidoxime) (PAO) is critical for optimizing amidoximation conditions, which determine the physicochemical properties and adsorption capabilities of PAO-based materials. Although the optimization of amidoximation conditions can be reported in the literature, a detailed research on the transformation is still missing. Herein, the effect of the amidoximation conditions (i.e. temperature, time, and NH2OH concentration) on the physicochemical properties and adsorption capabilities of PAO was studied in detail. The results showed that the extent of amidoximation reaction increased with increasing temperature, time, and NH2OH concentration. However, a considerably high temperature (>60 °C) and a considerably long time (>3 h) could result in the degradation and decomposition of PAO's surface topologies and functional groups, and then decrease its adsorption capability for U(vi). The optimal amidoximation condition was 3 h, 60 °C and 50 g L-1 NH2OH. At this condition, the PAO obtained presented the highest adsorption capability for U(vi) under experimental conditions. These results provide pivotal information on the transformation of PAO-based materials during the amidoximation process.

Rapid solidification of Sr-contaminated soil by consecutive microwave sintering: mechanism and stability evaluation.

Consecutive microwave sintering is a method proposed in this study to dispose soil contaminated by Sr during a nuclear accident by rapidly solidifying the contaminated soil. The results show that soil contaminated with 20 wt% SrSO4 and 30 wt% SrSO4 can be completely solidified by microwave sintering at 1100-1200 and 1300 â„ƒ, respectively, for 30 min. Sr was found to be cured into slawsonite (SrAl2Si2O8) and glass structures. Moreover, soil sintered at 1300 â„ƒ has large cured solubility (30 wt.%), good uniformity, and excellent hardness (6.9-7.2 GPa) and chemical durability (below 1.46 × 10-5 g m-2 d-1 at 28 d). Thus, consecutive microwave sintering technology may provide a new method for treating Sr-contaminated soil in case of a nuclear accident emergency.

A review of biopolymer (Poly-ß-hydroxybutyrate) synthesis in microbes cultivated on wastewater.

The large quantities of non-degradable single use plastics, production and disposal, in addition to increasing amounts of municipal and industrial wastewaters are among the major global issues known today. Biodegradable plastics from biopolymers such as Poly-ß-hydroxybutyrates (PHB) produced by microorganisms are potential substitutes for non-degradable petroleum-based plastics. This paper reviews the current status of wastewater-cultivated microbes utilized in PHB production, including the various types of wastewaters suitable for either pure or mixed culture PHB production. PHB-producing strains that have the potential for commercialization are also highlighted with proposed selection criteria for choosing the appropriate PHB microbe for optimization of processes. The biosynthetic pathways involved in producing microbial PHB are also discussed to highlight the advancements in genetic engineering techniques. Additionally, the paper outlines the factors influencing PHB production while exploring other metabolic pathways and metabolites simultaneously produced along with PHB in a bio-refinery context. Furthermore, the paper explores the effects of extraction methods on PHB yield and quality to ultimately facilitate the commercial production of biodegradable plastics. This review uniquely discusses the developments in research on microbial biopolymers, specifically PHB and also gives an overview of current commercial PHB companies making strides in cutting down plastic pollution and greenhouse gases.

Harvesting the vibration energy of α-MnO2 nanostructures for complete catalytic oxidation of carcinogenic airborne formaldehyde at ambient temperature.

Vibration is one of the most prevalent energy sources in natural environment, which can also be harvested and utilized to drive chemical reaction. Herein, mechanical vibration is used for enhancing the catalytic decomposition of formaldehyde at ambient temperature with the assistance of four well-defined morphologies α-MnO2 (nanowire, nanotube, nanorod and nanoflower). In particular, α-MnO2 nanowire exhibits the best catalytic activity, which can completely mineralize formaldehyde into carbon dioxide at ambient temperature by harvesting the vibration energy. To the best of our knowledge, this may be the first report that α-MnO2, as a non-noble metal catalyst, can completely decompose formaldehyde to carbon dioxide at ambient temperature. The characterization results show that α-MnO2 nanowire has a much higher oxygen vacancy concentration than other three catalysts. In addition, thermal effect generated from friction between nanoparticles induced by ultrasonic vibration may enhance its catalytic activity. More importantly, it is the vibration that effectively promotes the activation of O2 adsorbed on the surface oxygen vacancy to produce more , thus increasing the catalytic decomposition performance. The strategy presented herein demonstrates a new approach for efficient use of mechanical vibration to improve catalytic activity of traditional catalysts.